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FDA 510(k)

SUN KING

K-Number: K853752 · 1985-10-21

ApplicantAmerican Chase Company, Inc.
Decision Date1985-10-21
Product CodeFTC
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SUN KING is the device name listed in this FDA 510(k) record. The listed applicant is American Chase Company, Inc.. It received FDA 510(k) clearance on 1985-10-21 under 510(k) number K853752. The device is classified under product code FTC. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SUN KING?

SUN KING is a medical device that received FDA 510(k) clearance on 1985-10-21. The listed applicant is American Chase Company, Inc.. The 510(k) number is K853752.

When did SUN KING receive FDA 510(k) clearance?

SUN KING received FDA 510(k) clearance on 1985-10-21, under 510(k) number K853752.

Who is the listed applicant for SUN KING?

The FDA 510(k) record lists American Chase Company, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SUN KING?

The FDA product code for SUN KING is FTC.

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Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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